Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Fibrosis and KRT8[original query] |
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An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion. BMC medical genetics 2011 12 (1): 62. Stanke Frauke, Hedtfeld Silke, Becker Tim, Tümmler Burkha |
Non-coding keratin variants associate with liver fibrosis progression in patients with hemochromatosis. PloS one 2012 7 (3): e32669. Strnad Pavel, Kucukoglu Ozlem, Lunova Mariia, Guldiken Nurdan, Lienau Tim C, Stickel Felix, Omary M Bis |
Targeted Gene Next-Generation Sequencing in Chinese Children with Chronic Pancreatitis and Acute Recurrent Pancreatitis. The Journal of pediatrics 2017 11 191 158-163.e3. Xiao Yuan, Yuan Wentao, Yu Bo, Guo Yan, Xu Xu, Wang Xinqiong, Yu Yi, Yu Yi, Gong Biao, Xu Chun |
Trans-heterozygosity for mutations enhances the risk of recurrent/chronic pancreatitis in patients with Cystic Fibrosis. Molecular medicine (Cambridge, Mass.) 2018 Jul 24 (1): 38. Sofia Valentina Maria, Surace Cecilia, Terlizzi Vito, Da Sacco Letizia, Alghisi Federico, Angiolillo Antonella, Braggion Cesare, Cirilli Natalia, Colombo Carla, Di Lullo Antonella, Padoan Rita, Quattrucci Serena, Raia Valeria, Tuccio Giuseppe, Zarrilli Federica, Tomaiuolo Anna Cristina, Novelli Antonio, Lucidi Vincenzina, Lucarelli Marco, Castaldo Giuseppe, Angioni Adria |
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- Page last updated:Apr 16, 2024
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